BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 3737334)

  • 1. [Coffin-Siris syndrome].
    Bochkova DN; Ternova TI; Mastrakova VN
    Pediatriia; 1986 May; (5):59-61. PubMed ID: 3737334
    [No Abstract]   [Full Text] [Related]  

  • 2. Childhood Autism in a female with Coffin Siris Syndrome.
    Hersh JH; Bloom AS; Weisskopf B
    J Dev Behav Pediatr; 1982 Dec; 3(4):249-52. PubMed ID: 7153373
    [No Abstract]   [Full Text] [Related]  

  • 3. The Genée-Wiedemann syndrome, an acrofacial dysostosis--further observation.
    Opitz JM; Stickler GB
    Am J Med Genet; 1987 Aug; 27(4):971-5. PubMed ID: 3425606
    [No Abstract]   [Full Text] [Related]  

  • 4. [Coffin-Siris syndrome. Review of the literature].
    Quintana Herrera C; García Nieto VM; Duque Fernández MR; Morales Fernández MC; Hernández Rodríguez MC; Torres Lana A
    An Esp Pediatr; 1993 Jul; 39(1):53-7. PubMed ID: 8363153
    [No Abstract]   [Full Text] [Related]  

  • 5. Medulloblastoma in association with the Coffin-Siris syndrome.
    Rogers L; Pattisapu J; Smith RR; Parker P
    Childs Nerv Syst; 1988 Feb; 4(1):41-4. PubMed ID: 2456854
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Cranio-carpo-tarsal dysplasia or the whistling face syndrome (author's transl)].
    de la Peña J; de Torres ; Bonastre García F; Serrano JL; Crespo Valero C
    An Esp Pediatr; 1974; 7(5):452-7. PubMed ID: 4218458
    [No Abstract]   [Full Text] [Related]  

  • 7. [The Coffin-Siris syndrome. A new syndrome of mental retardation, hypo-aplasia of the nails and terminal phalanges of the 5th fingers and toes].
    Mastroiacovo P; Salvaggio E; Parenti D
    Minerva Pediatr; 1977 Mar; 29(11):773-8. PubMed ID: 875947
    [No Abstract]   [Full Text] [Related]  

  • 8. [Coffin-Siris syndrome. Critical study of the literature apropos of a case].
    Foasso MF; Hermier M; Descos B; Collet JP; Perron F
    Pediatrie; 1983 Mar; 38(2):111-7. PubMed ID: 6622139
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [The Coffin-Siris syndrome. Case report].
    Giovannucci Uzielli ML; Seminara S; Nicòtina PA; Consumi I; La Cauza C
    Minerva Pediatr; 1980 Feb; 32(4):245-54. PubMed ID: 6770244
    [No Abstract]   [Full Text] [Related]  

  • 10. Robin sequence and oligodactyly in mother and son--probably a further example of the postaxial acrofacial dysostosis syndrome.
    Meinecke P; Wiedemann HR
    Am J Med Genet; 1987 Aug; 27(4):953-7. PubMed ID: 3425604
    [No Abstract]   [Full Text] [Related]  

  • 11. A particular form of cranio-facio-mandibular dysostosis with type B brachydactylia.
    Van Damme W; Touitou D
    J Belge Radiol; 1980; 63(4):491-6. PubMed ID: 7204325
    [No Abstract]   [Full Text] [Related]  

  • 12. [Syndrome of broad thumbs with mental retardation in 2 infants. Rubinstein-Taybi syndrome].
    Dzvoníková Z; Lysá G
    Cesk Pediatr; 1968 Aug; 23(8):734-7. PubMed ID: 4386568
    [No Abstract]   [Full Text] [Related]  

  • 13. [On the differential diagnosis of bird's head dwarfism and Rubinstein-Taybi syndrome].
    Heinisch HM
    Radiologe; 1967 Dec; 7(12):387-90. PubMed ID: 5589760
    [No Abstract]   [Full Text] [Related]  

  • 14. Females with de novo aberrations in PHF6: clinical overlap of Borjeson-Forssman-Lehmann with Coffin-Siris syndrome.
    Zweier C; Rittinger O; Bader I; Berland S; Cole T; Degenhardt F; Di Donato N; Graul-Neumann L; Hoyer J; Lynch SA; Vlasak I; Wieczorek D
    Am J Med Genet C Semin Med Genet; 2014 Sep; 166C(3):290-301. PubMed ID: 25099957
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Analysis of phenotypic variability of Zimmermann-Laband syndrome].
    Il'ina EG; Lur'e IV; Vasiliauskene IP
    Pediatriia; 1988; (4):86-8. PubMed ID: 3205658
    [No Abstract]   [Full Text] [Related]  

  • 16. Aarskog's syndrome.
    Maxwell GM
    Med J Aust; 1982 Jul; 2(2):66-7. PubMed ID: 7121364
    [No Abstract]   [Full Text] [Related]  

  • 17. [Crouzon's craniofacial dysostosis with digital anomalies. Casuistic contribution].
    Manns KJ; Bopp KP
    Med Klin; 1965 Nov; 60(47):1899-903. PubMed ID: 5882911
    [No Abstract]   [Full Text] [Related]  

  • 18. The Greig cephalopolysyndactyly syndrome in a Canadian family.
    Chudley AE; Houston CS
    Am J Med Genet; 1982 Nov; 13(3):269-76. PubMed ID: 6295159
    [No Abstract]   [Full Text] [Related]  

  • 19. Choanal atresia in two unrelated patients with the Coffin-Siris syndrome.
    de Jong G; Nelson MM
    Clin Genet; 1992 Dec; 42(6):320-2. PubMed ID: 1493645
    [No Abstract]   [Full Text] [Related]  

  • 20. [Joint occurrence of congenital ring constrictions and limb amputations with craniofactial dysmorphia (author's transl)].
    Kereszty M; Földes G
    Monatsschr Kinderheilkd (1902); 1979 Feb; 127(2):104-6. PubMed ID: 763240
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.